One Raw material failed assay test is there any chance for failing purity of that material ?
7 12588Why we are use 0.005M Sulphuric acid, in control of absorbance performance test UV Spectrophotometer calibration
2 15559How much sample concentration should i inject against diluted standard in related substances for drug product in hplc analysis
1 3958Post New Analytical Chemistry Questions
why we should take dst factor for below 1%moisture samples
if peak get problamatic then what require to do?
Identify problem faced when mass spectroscopy is used with HPLC system ?
Principle of single pan analytical balance
How to calculation of residual solvent methanol (3000 ppm) standard solution, and how many quantity used of test sample
Difference between the quantitative analysis and qualitative analysis?
How to decide assay range for non pharmacopeial API analysis by HPLC? Could you give me any reference for same e.g Guidelines or Paper publications?
AT WHAT CONDITIONS WILL YOU ANALYSE A SAMPLE,WHICH ARE PRESERVED AT OTHER THAN THE AMBIENT CONDITIONS?(ie COLD STORAGE SAMPLES BELOW 20* CENTIGRADE?
In which situation we require to analytical method validation of excipient?
Is it nessesary all multimedia dissolution require descriminatory?
How can we calculate offset value pH measurment
why salisylic acid not using now days for disdolution calibration?
how we can identify the impurity is coming below loq at transfering site?
A ha tc is actual defination of retention time?
What is the difference between chromatographic purity and related substances?